SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12584340A= , CM000665.2:g.12584340A= | GRCh38 |
| NC_000003.11:g.12625839A= , CM000665.1:g.12625839A= | GRCh37 |
| NC_000003.10:g.12600839A= | NCBI36 |
| NG_007467.1:g.84840T= , LRG_413:g.84840T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*1786T= (RAF1) | ENSP00000401088.1:n.*1786T= | |
| ENST00000432427.3:c.1438T= (RAF1) | ||
| ENST00000460610.2:n.6433T= (RAF1) | ||
| ENST00000471449.2:n.931T= (RAF1) | ||
| ENST00000475353.2:n.4401T= (RAF1) | ||
| ENST00000684903.1:c.*1798T= (RAF1) | ENSP00000508612.1:n.*1798T= | |
| ENST00000685348.1:c.*1832T= (RAF1) | ENSP00000510285.1:n.*1832T= | |
| ENST00000685437.1:c.*174T= (RAF1) | ENSP00000508794.1:n.*174T= | |
| ENST00000685653.1:c.*174T= (RAF1) | ENSP00000509968.1:n.*174T= | |
| ENST00000685697.1:n.2856T= (RAF1) | ||
| ENST00000685738.1:c.*1085T= (RAF1) | ENSP00000510156.1:n.*1085T= | |
| ENST00000686409.1:n.5530T= (RAF1) | ||
| ENST00000686455.1:n.4842T= (RAF1) | ||
| ENST00000686762.1:c.*680T= (RAF1) | ENSP00000509767.1:n.*680T= | |
| ENST00000687257.1:n.4575T= (RAF1) | ||
| ENST00000687326.1:c.*3413T= (RAF1) | ENSP00000509665.1:n.*3413T= | |
| ENST00000687505.1:n.2239T= (RAF1) | ||
| ENST00000687923.1:c.*174T= (RAF1) | ENSP00000510255.1:n.*174T= | |
| ENST00000688269.1:n.2717T= (RAF1) | ||
| ENST00000688444.1:n.4238T= (RAF1) | ||
| ENST00000688543.1:c.*174T= (RAF1) | ENSP00000509612.1:n.*174T= | |
| ENST00000688625.1:c.*3490T= (RAF1) | ENSP00000509522.1:n.*3490T= | |
| ENST00000688803.1:n.3549T= (RAF1) | ||
| ENST00000689097.1:c.*1798T= (RAF1) | ENSP00000509756.1:n.*1798T= | |
| ENST00000689389.1:c.*174T= (RAF1) | ENSP00000510213.1:n.*174T= | |
| ENST00000689418.1:c.*4016T= (RAF1) | ENSP00000509467.1:n.*4016T= | |
| ENST00000689540.1:n.4489T= (RAF1) | ||
| ENST00000689876.1:c.*670T= (RAF1) | ENSP00000508535.1:n.*670T= | |
| ENST00000689914.1:c.*1055T= (RAF1) | ENSP00000509847.1:n.*1055T= | |
| ENST00000690397.1:c.*174T= (RAF1) | ENSP00000508730.1:n.*174T= | |
| ENST00000690460.1:c.*174T= (RAF1) | ENSP00000509106.1:n.*174T= | |
| ENST00000690585.1:c.847T= (RAF1) | ||
| ENST00000690625.1:n.3157T= (RAF1) | ||
| ENST00000691396.1:c.*1993T= (RAF1) | ENSP00000510712.1:n.*1993T= | |
| ENST00000691643.1:n.3174T= (RAF1) | ||
| ENST00000691724.1:c.*1078T= (RAF1) | ENSP00000509255.1:n.*1078T= | |
| ENST00000691779.1:c.*1699T= (RAF1) | ENSP00000508592.1:n.*1699T= | |
| ENST00000691888.1:c.995T= (RAF1) | ||
| ENST00000691899.1:c.*174T= (RAF1) | ENSP00000508763.1:n.*174T= | |
| ENST00000692069.1:n.5045T= (RAF1) | ||
| ENST00000692093.1:c.*174T= (RAF1) | ENSP00000509669.1:n.*174T= | |
| ENST00000692311.1:n.2945T= (RAF1) | ||
| ENST00000692558.1:n.4704T= (RAF1) | ||
| ENST00000692773.1:c.*1858T= (RAF1) | ENSP00000509055.1:n.*1858T= | |
| ENST00000692830.1:c.*1866T= (RAF1) | ENSP00000509461.1:n.*1866T= | |
| ENST00000693312.1:c.*174T= (RAF1) | ENSP00000508686.1:n.*174T= | |
| ENST00000693664.1:c.*572T= (RAF1) | ENSP00000509614.1:n.*572T= | |
| ENST00000693705.1:c.*1500T= (RAF1) | ENSP00000510697.1:n.*1500T= | |
| ENST00000251849.9:c.*174T= (RAF1) MANE Select | ENSP00000251849.4:n.*174T= | |
| ENST00000442415.7:c.*174T= (RAF1) | ENSP00000401888.2:n.*174T= | |
| ENST00000676541.1:c.*2087A= (MKRN2) | ENSP00000503730.1:n.*2087A= | |
| ENST00000677142.1:c.*2087A= (MKRN2) | ENSP00000504455.1:n.*2087A= | |
| ENST00000677816.1:c.*642A= (MKRN2) | ENSP00000502893.1:n.*642A= | |
| ENST00000677941.1:n.2150A= (MKRN2) | ||
| ENST00000251849.8:c.*174T= (RAF1) | ENSP00000251849.4:n.*174T= | |
| ENST00000423275.5:c.*1798T= (RAF1) | ENSP00000401088.1:n.*1798T= | |
| ENST00000432427.2:c.1758T= (RAF1) | ENSP00000398591.2:n.1758T= | |
| ENST00000442415.6:c.*174T= (RAF1) | ENSP00000401888.2:n.*174T= | |
| NM_002880.3:c.*174T= , LRG_413t1:c.*174T= (RAF1) | NP_002871.1:n.*174T= | |
| XM_005265355.1:c.*174T= (RAF1) | XP_005265412.1:n.*174T= | |
| XM_005265357.1:c.*174T= (RAF1) | XP_005265414.1:n.*174T= | |
| XM_005265358.3:c.*174T= (RAF1) | XP_005265415.1:n.*174T= | |
| XM_005265359.3:c.*174T= (RAF1) | XP_005265416.1:n.*174T= | |
| XM_011533974.1:c.*174T= (RAF1) | XP_011532276.1:n.*174T= | |
| XM_011533975.1:c.*174T= (RAF1) | XP_011532277.1:n.*174T= | |
| NM_001354689.1:c.*174T= (RAF1) | NP_001341618.1:n.*174T= | |
| NM_001354690.1:c.*174T= (RAF1) | NP_001341619.1:n.*174T= | |
| NM_001354691.1:c.*174T= (RAF1) | NP_001341620.1:n.*174T= | |
| NM_001354692.1:c.*174T= (RAF1) | NP_001341621.1:n.*174T= | |
| NM_001354693.1:c.*174T= (RAF1) | NP_001341622.1:n.*174T= | |
| NM_001354694.1:c.*174T= (RAF1) | NP_001341623.1:n.*174T= | |
| NM_001354695.1:c.*174T= (RAF1) | NP_001341624.1:n.*174T= | |
| NR_148940.1:n.2649T= (RAF1) | ||
| NR_148941.1:n.2595T= (RAF1) | ||
| NR_148942.1:n.2534T= (RAF1) | ||
| XM_011533974.3:c.*174T= (RAF1) | XP_011532276.1:n.*174T= | |
| XM_017006966.1:c.*174T= (RAF1) | XP_016862455.1:n.*174T= | |
| NM_001354689.3:c.*174T= (RAF1) | NP_001341618.1:n.*174T= | |
| NM_001354690.2:c.*174T= (RAF1) | NP_001341619.1:n.*174T= | |
| NM_001354691.2:c.*174T= (RAF1) | NP_001341620.1:n.*174T= | |
| NM_001354692.2:c.*174T= (RAF1) | NP_001341621.1:n.*174T= | |
| NM_001354693.2:c.*174T= (RAF1) | NP_001341622.1:n.*174T= | |
| NM_001354694.2:c.*174T= (RAF1) | NP_001341623.1:n.*174T= | |
| NM_001354695.2:c.*174T= (RAF1) | NP_001341624.1:n.*174T= | |
| NR_148940.2:n.2565T= (RAF1) | ||
| NR_148941.2:n.2511T= (RAF1) | ||
| NR_148942.2:n.2450T= (RAF1) | ||
| NM_001354690.3:c.*174T= (RAF1) | NP_001341619.1:n.*174T= | |
| NM_001354691.3:c.*174T= (RAF1) | NP_001341620.1:n.*174T= | |
| NM_001354692.3:c.*174T= (RAF1) | NP_001341621.1:n.*174T= | |
| NM_001354693.3:c.*174T= (RAF1) | NP_001341622.1:n.*174T= | |
| NM_001354694.3:c.*174T= (RAF1) | NP_001341623.1:n.*174T= | |
| NM_001354695.3:c.*174T= (RAF1) | NP_001341624.1:n.*174T= | |
| NM_002880.4:c.*174T= (RAF1) MANE Select | NP_002871.1:n.*174T= | |
| NR_148940.3:n.2565T= (RAF1) | ||
| NR_148941.3:n.2511T= (RAF1) | ||
| NR_148942.3:n.2450T= (RAF1) |